{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T12:39:39Z","timestamp":1789994379143,"version":"4.0.1"},"reference-count":40,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2021,4,1]],"date-time":"2021-04-01T00:00:00Z","timestamp":1617235200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,4,1]],"date-time":"2021-04-01T00:00:00Z","timestamp":1617235200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2021,4,1]],"date-time":"2021-04-01T00:00:00Z","timestamp":1617235200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2021,4,1]],"date-time":"2021-04-01T00:00:00Z","timestamp":1617235200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2021,4,1]],"date-time":"2021-04-01T00:00:00Z","timestamp":1617235200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2021,4,1]],"date-time":"2021-04-01T00:00:00Z","timestamp":1617235200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2021,4,1]],"date-time":"2021-04-01T00:00:00Z","timestamp":1617235200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"funder":[{"DOI":"10.13039\/501100001409","name":"Department of Science and Technology, Ministry of Science and Technology, India","doi-asserted-by":"publisher","award":["DST\/CSRI\/PDF-21\/2018"],"award-info":[{"award-number":["DST\/CSRI\/PDF-21\/2018"]}],"id":[{"id":"10.13039\/501100001409","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001409","name":"Department of Science and Technology, Ministry of Science and Technology, India","doi-asserted-by":"publisher","award":["DST\/CSRI-P\/2017\/22 &amp; SR\/CSRI\/PDF-32\/2014"],"award-info":[{"award-number":["DST\/CSRI-P\/2017\/22 &amp; SR\/CSRI\/PDF-32\/2014"]}],"id":[{"id":"10.13039\/501100001409","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Neuroscience Letters"],"published-print":{"date-parts":[[2021,4]]},"DOI":"10.1016\/j.neulet.2021.135816","type":"journal-article","created":{"date-parts":[[2021,3,9]],"date-time":"2021-03-09T17:54:31Z","timestamp":1615312471000},"page":"135816","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":16,"special_numbering":"C","title":["Identification of GBA mutations among neurodegenerative disease patients from eastern India"],"prefix":"10.1016","volume":"751","author":[{"given":"Arindam","family":"Biswas","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dipanwita","family":"Sadhukhan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5696-9839","authenticated-orcid":false,"given":"Atanu","family":"Biswas","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shyamal K.","family":"Das","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tapas K","family":"Banerjee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Partha Sarathi","family":"Bal","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sandip","family":"Pal","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amitabha","family":"Ghosh","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kunal","family":"Ray","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jharna","family":"Ray","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.neulet.2021.135816_bib0005","doi-asserted-by":"crossref","first-page":"1215","DOI":"10.1016\/j.parkreldis.2014.09.003","article-title":"Glucocerebrosidase mutations in primary parkinsonism","volume":"20","author":"Asselta","year":"2014","journal-title":"Parkinsonism Relat. Disord."},{"key":"10.1016\/j.neulet.2021.135816_bib0010","doi-asserted-by":"crossref","first-page":"540","DOI":"10.1177\/1073858417748875","article-title":"Glucocerebrosidase and Parkinson Disease, Molecular, Clinical and Therapeutic Implications","volume":"5","author":"Balestrino","year":"2018","journal-title":"Neuroscientist"},{"key":"10.1016\/j.neulet.2021.135816_bib0015","doi-asserted-by":"crossref","first-page":"578","DOI":"10.1001\/archneurol.2009.54","article-title":"Association of glucocerebrosidase mutations with dementia with lewy bodies","volume":"66","author":"Clark","year":"2009","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.neulet.2021.135816_bib0020","doi-asserted-by":"crossref","first-page":"986","DOI":"10.1016\/j.parkreldis.2014.06.007","article-title":"Glucocerebrosidase mutations in Thai patients with Parkinson\u2019s disease","volume":"20","author":"Pulkes","year":"2014","journal-title":"Parkinsonism Relat. Disord."},{"key":"10.1016\/j.neulet.2021.135816_bib0025","doi-asserted-by":"crossref","first-page":"392","DOI":"10.1093\/brain\/aws318","article-title":"Glucocerebrosidase mutations influence the natural history of Parkinson\u2019s disease in a community-based incident cohort","volume":"136","author":"Winder-Rhodes","year":"2013","journal-title":"Brain."},{"key":"10.1016\/j.neulet.2021.135816_bib0030","doi-asserted-by":"crossref","first-page":"e523","DOI":"10.1212\/NXG.0000000000000523","article-title":"The SPID-GBA study: sex distribution, penetrance, incidence, and dementia in GBA-PD","volume":"6","author":"Straniero","year":"2020","journal-title":"Neurol. Genet."},{"key":"10.1016\/j.neulet.2021.135816_bib0035","doi-asserted-by":"crossref","first-page":"1944","DOI":"10.1212\/WNL.0b013e3182735e9a","article-title":"GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology","volume":"79","author":"Tsuang","year":"2012","journal-title":"Neurology."},{"key":"10.1016\/j.neulet.2021.135816_bib0040","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1002\/ajmg.1320440328","article-title":"Mutation analysis in Gaucher disease","volume":"44","author":"Beutler","year":"1992","journal-title":"Am. J. Med. Genet."},{"key":"10.1016\/j.neulet.2021.135816_bib0045","article-title":"A meta-analysis of GBA-Related clinical symptoms in parkinson\u2019s disease","volume":"2018","author":"Zhang","year":"2018","journal-title":"Parkinsons Dis."},{"key":"10.1016\/j.neulet.2021.135816_bib0050","doi-asserted-by":"crossref","first-page":"43","DOI":"10.3389\/fnmol.2018.00043","article-title":"Integrated genetic analysis of racial differences of common GBA variants in parkinson\u2019s disease: a meta-analysis","volume":"11","author":"Zhang","year":"2018","journal-title":"Front. Mol. Neurosci."},{"key":"10.1016\/j.neulet.2021.135816_bib0055","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1016\/j.neulet.2012.02.035","article-title":"Association of mutations in the glucocerebrosidase gene with Parkinson disease in a Korean population","volume":"514","author":"Choi","year":"2012","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.neulet.2021.135816_bib0060","doi-asserted-by":"crossref","first-page":"791","DOI":"10.1002\/mds.26562","article-title":"Lysosomal dysfunction and \u03b1-Synuclein aggregation in parkinson\u2019s disease: diagnostic links","volume":"31","author":"Moors","year":"2016","journal-title":"Mov. Disord."},{"key":"10.1016\/j.neulet.2021.135816_bib0065","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1186\/1750-1172-9-86","article-title":"Parkin-mediated ubiquitination of mutant glucocerebrosidase leads to competition with its substrates PARIS and ARTS","volume":"9","author":"Bendikov-Bar","year":"2014","journal-title":"Orphanet J. Rare Dis."},{"key":"10.1016\/j.neulet.2021.135816_bib0070","doi-asserted-by":"crossref","first-page":"630","DOI":"10.1177\/1533317514531442","article-title":"Dementia and cognitive impairment in patients with Parkinson\u2019s disease from India: a 7-year prospective study","volume":"29","author":"Sanyal","year":"2014","journal-title":"Am. J. Alzheimers Dis. Other Demen."},{"key":"10.1016\/j.neulet.2021.135816_bib0075","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1159\/000329862","article-title":"Subtypes of dementia: a study from a memory clinic in India","volume":"32","author":"Alladi","year":"2011","journal-title":"Dement. Geriatr. Cogn. Disord."},{"key":"10.1016\/j.neulet.2021.135816_bib0080","doi-asserted-by":"crossref","DOI":"10.1155\/2015\/916971","article-title":"Effect of GBA mutations on phenotype of parkinson\u2019s disease: a study on chinese population and a meta-analysis","author":"Zhang","year":"2015","journal-title":"Parkinsons Dis."},{"key":"10.1016\/j.neulet.2021.135816_bib0085","doi-asserted-by":"crossref","first-page":"634","DOI":"10.1002\/mds.25857","article-title":"The neurobiological basis of cognitive impairment in Parkinson\u2019s disease","volume":"29","author":"Halliday","year":"2014","journal-title":"Mov. Disord."},{"key":"10.1016\/j.neulet.2021.135816_bib0090","doi-asserted-by":"crossref","first-page":"1649","DOI":"10.4103\/0028-3886.246249","article-title":"Genetic analysis of the glucocerebrosidase gene in South Indian patients with Parkinson\u2019s disease","volume":"66","author":"Yadav","year":"2018","journal-title":"Neurol. India"},{"key":"10.1016\/j.neulet.2021.135816_bib0095","doi-asserted-by":"crossref","first-page":"4","DOI":"10.4172\/2327-5790.1000144","article-title":"Screening of genetic mutations in GBA1, GIGYF2 and VPS35 in parkinson disease patients from India","volume":"5","author":"Halder","year":"2016","journal-title":"J. Genet Disor. Genet Rep."},{"key":"10.1016\/j.neulet.2021.135816_bib0100","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1016\/j.parkreldis.2020.07.014","article-title":"Novel and reported variants in Parkinson\u2019s disease genes confer high disease burden among Indians","volume":"78","author":"Kumar","year":"2020","journal-title":"Parkinsonism Relat. Disord."},{"key":"10.1016\/j.neulet.2021.135816_bib0105","first-page":"37","article-title":"An urban community-based study of cognitive function among non-demented elderly population in India","volume":"11","author":"Das","year":"2016","journal-title":"Neurol. Asia"},{"key":"10.1016\/j.neulet.2021.135816_bib0110","article-title":"Clinical and radiological profile of posterior cortical atrophy and comparison with a group of typical Alzheimer disease and amnestic mild cognitive impairment","author":"Das","year":"2020","journal-title":"Acta. Neurol. Belg."},{"key":"10.1016\/j.neulet.2021.135816_bib0115","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1016\/0003-2697(89)90430-2","article-title":"Purification of human genomic DNA from whole blood using sodium perchlorate in place of phenol","volume":"180","author":"Johns","year":"1989","journal-title":"Anal. Biochem."},{"key":"10.1016\/j.neulet.2021.135816_bib0120","doi-asserted-by":"crossref","first-page":"202","DOI":"10.1093\/hmg\/ddq454","article-title":"French parkinson\u2019s Disease Genetics Study Group. Large-scale screening of the gaucher\u2019s disease-related glucocerebrosidase gene in Europeans with parkinson\u2019s disease","volume":"20","author":"Lesage","year":"2011","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.neulet.2021.135816_bib0125","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1016\/j.cell.2011.06.001","article-title":"Gaucher disease glucocerebrosidase and \u03b1-synuclein form a bidirectional pathogenic loop in synucleinopathies","volume":"146","author":"Mazzulli","year":"2011","journal-title":"Cell."},{"key":"10.1016\/j.neulet.2021.135816_bib0130","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1038\/nchembio850","article-title":"Structure of acid beta-glucosidase with pharmacological chaperone provides insight into Gaucher disease","volume":"3","author":"Lieberman","year":"2007","journal-title":"Nat. Chem. Biol."},{"key":"10.1016\/j.neulet.2021.135816_bib0135","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1016\/j.neuint.2015.12.004","article-title":"Advances in GBA-associated Parkinson\u2019s disease--Pathology, presentation and therapies","volume":"93","author":"Barkhuizen","year":"2016","journal-title":"Neurochem. Int."},{"key":"10.1016\/j.neulet.2021.135816_bib0140","doi-asserted-by":"crossref","first-page":"12101","DOI":"10.1073\/pnas.1108197108","article-title":"CNS expression of glucocerebrosidase corrects alpha-synuclein pathology and memory in a mouse model of Gaucher-related synucleinopathy","volume":"108","author":"Sardi","year":"2011","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.neulet.2021.135816_bib0145","doi-asserted-by":"crossref","first-page":"575","DOI":"10.1007\/s12035-012-8340-3","article-title":"The role of glia in \u03b1-synucleinopathies","volume":"47","author":"Fellner","year":"2013","journal-title":"Mol. Neurobiol."},{"key":"10.1016\/j.neulet.2021.135816_bib0150","doi-asserted-by":"crossref","first-page":"727","DOI":"10.1001\/jamaneurol.2013.1925","article-title":"A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies","volume":"70","author":"Nalls","year":"2013","journal-title":"JAMA Neurol."},{"key":"10.1016\/j.neulet.2021.135816_bib0155","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1016\/j.parkreldis.2010.09.009","article-title":"Glucocerebrosidase mutations in diffuse Lewy body disease","volume":"17","author":"Nishioka","year":"2011","journal-title":"Parkinsonism Relat. Disord."},{"key":"10.1016\/j.neulet.2021.135816_bib0160","doi-asserted-by":"crossref","first-page":"609","DOI":"10.1016\/S1474-4422(13)70090-5","article-title":"Tau pathology and neurodegeneration","volume":"12","author":"Spillantini","year":"2013","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.neulet.2021.135816_bib0165","doi-asserted-by":"crossref","first-page":"e61","DOI":"10.1111\/ene.12086","article-title":"No association of GBA mutations and multiple system atrophy","volume":"20","author":"Srulijes","year":"2013","journal-title":"Eur. J. Neurol."},{"key":"10.1016\/j.neulet.2021.135816_bib0170","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1016\/j.jocn.2012.01.055","article-title":"Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China","volume":"20","author":"Sun","year":"2013","journal-title":"J. Clin. Neurosci."},{"key":"10.1016\/j.neulet.2021.135816_bib0175","doi-asserted-by":"crossref","first-page":"417","DOI":"10.1002\/acn3.185","article-title":"Variants associated with Gaucher disease in multiple system atrophy","volume":"2","author":"Mitsui","year":"2015","journal-title":"Ann. Clin. Transl. Neurol."},{"key":"10.1016\/j.neulet.2021.135816_bib0180","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0115747","article-title":"Glucocerebrosidase gene mutations associated with Parkinson\u2019s disease: a meta-analysis in a Chinese population","volume":"9","author":"Chen","year":"2014","journal-title":"PLoS One"},{"key":"10.1016\/j.neulet.2021.135816_bib0185","doi-asserted-by":"crossref","first-page":"977","DOI":"10.1136\/jnnp.2006.105940","article-title":"Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese","volume":"78","author":"Wu","year":"2007","journal-title":"J. Neurol. Neurosurg. Psychiatry."},{"key":"10.1016\/j.neulet.2021.135816_bib0190","doi-asserted-by":"crossref","first-page":"1005","DOI":"10.1002\/mds.23009","article-title":"Glucocerebrosidase Gene L444P mutation is a risk factor for Parkinson\u2019s disease in Chinese population","volume":"25","author":"Sun","year":"2010","journal-title":"Mov. Disord."},{"key":"10.1016\/j.neulet.2021.135816_bib0195","doi-asserted-by":"crossref","first-page":"256","DOI":"10.1016\/j.neulet.2009.12.007","article-title":"Association between GBA L444P mutation and sporadic parkinson\u2019s disease from Mainland China","volume":"469","author":"Mao","year":"2010","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.neulet.2021.135816_bib0200","doi-asserted-by":"crossref","first-page":"1227","DOI":"10.1111\/j.1468-1331.2011.03362.x","article-title":"Contribution of glucocerebrosidase mutation in a large cohort of sporadic Parkinson\u2019s disease in Taiwan","volume":"18","author":"Huang","year":"2011","journal-title":"Eur. J. Neurol."}],"container-title":["Neuroscience Letters"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0304394021001944?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0304394021001944?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,4,30]],"date-time":"2026-04-30T12:46:40Z","timestamp":1777553200000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0304394021001944"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,4]]},"references-count":40,"alternative-id":["S0304394021001944"],"URL":"https:\/\/doi.org\/10.1016\/j.neulet.2021.135816","relation":{},"ISSN":["0304-3940"],"issn-type":[{"value":"0304-3940","type":"print"}],"subject":[],"published":{"date-parts":[[2021,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Identification of GBA mutations among neurodegenerative disease patients from eastern India","name":"articletitle","label":"Article Title"},{"value":"Neuroscience Letters","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.neulet.2021.135816","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2021 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}],"article-number":"135816"}}